Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- befree-2016 importedOn "2016-02-19" NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_assertion wasGeneratedBy ECO_0000203 NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_assertion wasDerivedFrom befree-2016 NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_assertion SIO_000772 17525480 NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_assertion evidence source_evidence_literature NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_assertion description "[An intriguing hypothesis proposes that mutations of RET, NF1, VHL, or SDH predispose to hereditary pheochromocytoma/ paraganglioma by causing defective apoptotic culling of cells that would normally be destroyed during embryogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.